Aryloxymethylcarbonochloridate ester intermediates for use in synthesizing pro drugs and their use therefor

ABSTRACT

The present invention relates to hitherto unknown intermediate of formula, in which R 1  stands for hydrogen or a straight or branched aliphatic C 1  -C 20  carbon chain or an aryl or aralkyl group, aryl and &#34;ar&#34; meaning an aromatic or heterocyclic, 5- or 6-membered ring substituent containing 1 or 2 hetero atoms selected among O, S and N, R 1  optionally being further substituted, and its chain being interrupted by hetero atoms like oxygen, or by carbonyl group(s); and R 3  stands for hydrogen or C 1  -C 3  alkyl. The present intermediates can be used in a one step method for producing prodrugs of formula, where D-H =drug itself.

The present invention relates to hitherto unknown intermediates of the below formula I for use in the synthesis of prodrugs.

In recent years, chemical modification of drugs into labile derivatives (prodrugs) with improved physicochemical properties that enable better transport through biological barriers has become a useful approach for improving-drug delivery. Such transformation is often practised on ionizable molecules containing e.g. a carboxylic acid, an amino, or a hydroxy group that can be utilized for derivatization, in order to modify their ionization at physiological pH and to render desirable partition and solubility properties.

A necessary requirement of this approach is that the said prodrug is non-toxic and, when administered to a warm-blooded animal including a human being, is enzymatically and/or chemically cleaved in such a manner as to release the drug at its target or site of activity, quantitatively and at a desirable rate, while the remaining cleaved moiety remains non-toxic and is metabolized in such a manner that non-toxic metabolic products are produced.

It is, of course, also desirable that the prodrug can be provided without excessive costs in connection with its production, in particular without an appreciable loss of drug itself during its production and recovery, since the drug is usually the more expensive part of the prodrug.

The intermediate used to react with the drug in providing the prodrug should advantageously be stable and still be reasonably reactive.

In recent years, acyloxyalkoxycarbonyl derivatives have become interesting bioreversible prodrug moieties of drugs and medicaments which are more readily bioavailable than the drug itself, and further are less irritating to topical and gastric mucosal membranes and are more permeable through such membranes. An example of such prodrug is shown in the formula II ##STR1## where D-H=the drug (D-H containing an OH, SH, NH₂ or a monosubstituted N function), and R¹ COOH=non-toxic carboxylic acid, R¹ for instance meaning hydrogen or a straight or branched aliphatic C₁ -C₂₀ carbon chain or an aryl or aralkyl group, aryl and `ar` meaning an aromatic or heterocyclic, 5- or 6-membered ring substituent containing 1 or 2 hetero atoms selected among O, S and N. As examples of such aromatic or heterocyclic substituents, mention may be made of phenyl, furyl, thienyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, pyridyl, and pyrimidinyl. R¹ may be further substituted, and its chain be interrupted by hetero atoms like oxygen, or by carbonyl group(s). R³ means hydrogen or C₁ -C₃ alkyl. Esters of this type have for instance been used as prodrugs of R¹ COOH and have been shown to be enzymatically hydrolyzed in man. Obviously such esters will also liberate D-H.

Some esters of the formula II have been produced in a multi-step procedure, confer J. Med. Chem. 1988, 31, p. 318ff, where the drug (containing a primary or secondary amine group being the point of reaction) is reacted with a compound of formula III ##STR2## in which formula, R^(1') and R^(3') are hydrogen or lower alkyl.

The intermediates of formula III have the disadvantage of reacting rather slowly, if at all, when used in the production of prodrugs of formula II (Chemistry and Industry, 1967, p. 1960). Also, they seem to-be non crystalline and not very stable and are therefore difficult and costly to use technically (purification by chromatography).

It has now surprisingly turned out that intermediates of the formula I ##STR3## in which formula R¹ and R³ have the above meanings can be provided which are both stable and of high purity following simple distillation or recrystallization, and which are still very reactive so that they can be used in a one step method for producing the desired prodrugs of the formula II in a high purity and without appreciable loss of the drug itself which is normally the most expensive part of the prodrug.

The intermediates of formula I, in which R³ stands for hydrogen have been shown to be the more reactive and stable ones when used in the production of the desired prodrugs, and are thus the preferred ones according to the present invention.

It will be obvious to the man skilled in the art that, depending on the meaning of D or R¹ it may become necessary during the production of compounds of formula I or formula II to protect temporarily possible substituents reactive to acid chlorides and to remove the protective group(s) after reaction of I with D-H.

Also according to the invention, the intermediates of formula I (R³ =H) can be produced according to the following Scheme A (R¹ and R² having the above meanings) ##STR4## according to which the multifunctional chloromethyl carbonochloridate (3)--numbers in parentheses refer to numbers in the Scheme--is used as a starting material obtained by chlorination of methyl carbonochloridate or by treatment of formaldehyde with phosgene or with trichloromethyl carbonochloridate. The relationship between the reactivities of the two electrophilic centres in (3) is temporarily reversed by conversion of the acid chloride function to the less reactive carbonothioate group of (4). After utilization of the second chlorine atom for the formation of an ester (6), the acid chloride function of (7) (being the desired intermediate of formula I) is finally restored by chlorination.

It was known that the compound (3) could react with alcohols and phenols in the presence of pyridine to afford the derived alkyl or aryl chloromethyl carbonates, but this method did not work with alkylthiols. However, according to the present invention, when pyridine was replaced with a tertiary amine, such as triethylamine or diisopropylethylamine, and when an ethereal solution of a mercaptan R² SH and the tertiary amine was added to an ice-cold solution of (3) in ether, good to excellent yields (75-100%) of O-chloromethyl S-alkyl or S-aryl carbonothioates (4) could be obtained. Another possibility turned out to be the reaction of a suspension of R² SNa in ether with (3) affording varying yields (40-90%) of (4), the yields increasing with larger alkylthiols.

Before performing the reaction leading to an ester (6), the compound (4) was converted to its iodo analogue (5) by the Finkelstein reaction using sodium iodide at elevated temperature (40° C.), confer Scheme A, mostly in the presence of sodium hydrogen carbonate to neutralize traces of hydrogen iodide formed since addition of this base was found to preserve (5) from deterioration. Without this addition, (5b) became coloured in a few hours. Reaction in acetone at 40° C. for four hours with two equivalents of sodium iodide (and 0.1 equivalent of sodium hydrogen carbonate) was found to be optimal.

Due to their presumed instability, the crude liquid iodo compounds (5) obtained in almost quantitative yields were generally used immediately for the next step without any attempt at purification. However, the above mentioned addition of the preserving amount of the weak base showed to be sufficient to prevent deterioration of the iodo compounds, even when kept for years at -20° C.

The double esters (6) were mostly prepared by stirring a suspension of sodium carboxylate in dimethylformamide with the iodo compound (5) at room temperature for 20 hours. However, the use of liquid-liquid phase transfer conditions (method D in Scheme A) turned out to be the preferable method, the optimum being the addition for half an hour of the iodo ester (5) (R³ =H) at room temperature to a stirred mixture of tetrabutylammonium (TBA) hydrogen sulfate, sodium hydrogen carbonate, and carboxylic acid (1.3:2.6:1.3) in water and methylene chloride, 1,2-dichloroethane, or ethyl acetate followed by stirring for 1 hour. Simple carboxylic acids tend to give higher yields (80-100%) than carboxylic acids containing additional functional groups. Other methods are workable, confer e.g. Scheme A, methods E, F, and J (Examples 9, 10, and 14, respectively).

When purified by distillation, the double esters (6) were generally pure enough for subsequent conversion, in step 4 of Scheme A, to the desired intermediates (7) by restoring the acid chloride function through reaction with sulfuryl chloride, preferably in the presence of a catalytic amount of boron trifluoride etherate at -25°--30° C. and subsequent stirring at 0° C. for one hour and half an hour at room temperature. The distillable compounds (7) were produced in high yields and could be kept without deterioration for years in a refrigerator.

The synthetic sequence is not restricted to acyloxymethyl carbonochloridates. By substituting 1-chloroalkyl carbonochloridates for (3) and treating the derived O-1-chloroalkyl S-alkyl carbonothioate with TBA butanoate in tetrahydrofuran for a suitable period of time, followed by sulfuryl chloride treatment provided a solution of 1-butanoyloxyalkyl carbonochloridate, but these intermediates seem to be less stable than (7).

The present intermediates of formula I can generally be prepared by reacting a 1-haloalkyl carbonochloridate of the formula IV ##STR5## where R³ has the above meanings, is reacted with R² SR⁴, R² being C₁ -C₄ alkyl, and R⁴ being hydrogen or an alkali metal ion, to form a 1-haloalkyl carbonothioate of the formula V ##STR6## R² and R³ having the above meanings, which is transformed into a 1-acyloxyalkyl carbonothioate of the formula VI ##STR7## R¹, R² and R³ having the above meanings by reaction with a salt of a carboxylic acid R¹ COOH, R¹ having the above meanings, and finally reacting the compound of formula VI with a chlorinating agent to yield the desired intermediate of formula I.

If, in formula I, R³ =H, the present intermediates are preferably being prepared by converting the compound of formula V to the corresponding iodide by reaction with sodium iodide, before transforming it via VI to I.

The preferred chlorinating agent used in the final step of the preparation of the present intermediates is sulfuryl chloride.

As mentioned above, it has surprisingly turned out that the present intermediates of the formula I can be provided in good yields and of reasonable costs, that they are stable, and even very reactive, in their intended use in the production of prodrugs. Due to the polyfunctionality of the intermediates, and the known catalytic decomposition of simple alkyl carbonochloridates, acylation reactions like the one used in providing the desired prodrugs could be expected to be troublesome, but this turned out not to be so, as illustrated by the non-optimized reactions of I with a few hydroxyl or amino group containing compounds (Examples 16-21). The present intermediates are effective means in the production of the prodrugs in question, and they provide said final prodrugs in good yields in one step processes.

The invention shall in the following be further illustrated. The numbers and number/letter combinations used refer to Scheme A, to the Tables 1-10 and to the Examples given in the following.

    ______________________________________                                                (4-5)                                                                               R.sup.2                                                            ______________________________________                                                a    CH.sub.3                                                                  b    CH.sub.3 CH.sub.2                                                         c    CH.sub.3 (CH.sub.2).sub.3                                                 d                                                                                    ##STR8##                                                                 e                                                                                    ##STR9##                                                          ______________________________________                                         (6)    R.sup.1          R.sup.2                                                ______________________________________                                         ab     H                CH.sub.3 CH.sub.2                                      ba     CH.sub.3         CH.sub.3                                               bb     CH.sub.3         CH.sub.3 CH.sub.2                                      ca     CH.sub.3 CH.sub.2                                                                               CH.sub.3                                               cb     CH.sub.3 CH.sub.2                                                                               CH.sub.3 CH.sub.2                                      cc     CH.sub.3 CH.sub.2                                                                               CH.sub.3 (CH.sub.2).sub.3                              da     CH.sub.3 (CH.sub.2).sub.2                                                                       CH.sub.3                                               db     CH.sub.3 (CH.sub.2).sub.2                                                                       CH.sub.3 CH.sub.2                                      dd     CH.sub.3 (CH.sub.2).sub.2                                                                        ##STR10##                                             eb     CH.sub.3 (CH.sub.2).sub.3                                                                       CH.sub.3 CH.sub.2                                      fb     (CH.sub.3).sub.3 C                                                                              CH.sub.3 CH.sub.2                                      fc     (CH.sub.3).sub.3 C                                                                              CH.sub.3 (CH.sub.2).sub.3                              fe     (CH.sub.3).sub.3 C                                                                               ##STR11##                                             gb     CH.sub.3 (CH.sub.2).sub.4                                                                       CH.sub.3 CH.sub.2                                      hb     CH.sub.3 (CH.sub.2).sub.5                                                                       CH.sub.3 CH.sub.2                                      ib     CH.sub.3 (CH.sub.2).sub.6                                                                       CH.sub.3 CH.sub.2                                      jb     CH.sub.3 (CH.sub.2).sub.7                                                                       CH.sub.3 CH.sub.2                                      kb     CH.sub.3 (CH.sub.2).sub.12                                                                      CH.sub.3 CH.sub.2                                      lb                                                                                     ##STR12##       CH.sub.3 CH.sub.2                                      mb                                                                                     ##STR13##       CH.sub.3 CH.sub.2                                      nb                                                                                     ##STR14##       CH.sub.3 CH.sub.2                                      ob                                                                                     ##STR15##       CH.sub.3 CH.sub.2                                      pb                                                                                     ##STR16##       CH.sub.3 CH.sub.2                                      qb     CH.sub.3 CH.sub.2 OCH.sub.2                                                                     CH.sub.3 CH.sub.2                                      rb                                                                                     ##STR17##       CH.sub.3 CH.sub.2                                      sb     F.sub.3 C        CH.sub.3 CH.sub.2                                      tb                                                                                     ##STR18##       CH.sub.3 CH.sub.2                                      ub                                                                                     ##STR19##       CH.sub.3 CH.sub.2                                      ______________________________________                                                (7) R.sup.1                                                             ______________________________________                                                b   CH.sub.3                                                                   c   CH.sub.3 CH.sub.2                                                          d   CH.sub.3 (CH.sub.2).sub.2                                                  e   CH.sub.3 (CH.sub.2).sub.3                                                  f   (CH.sub.3).sub.3 C                                                         g   CH.sub.3 (CH.sub.2).sub.4                                                  h   CH.sub.3 (CH.sub.2).sub.5                                                  i   CH.sub.3 (CH.sub.2).sub.6                                                  j   CH.sub.3 (CH.sub.2).sub.7                                                  k   CH.sub.3 (CH.sub.2).sub.12                                                 l                                                                                   ##STR20##                                                                 m                                                                                   ##STR21##                                                                 o                                                                                   ##STR22##                                                                 p                                                                                   ##STR23##                                                                 q   CH.sub.3 CH.sub.2 OCH.sub.2                                                r                                                                                   ##STR24##                                                          ______________________________________                                         (8)       R.sup.1  Nu                                                          ______________________________________                                         c1        CH.sub.3 CH.sub.2                                                                        ##STR25##                                                  c2        CH.sub.3 CH.sub.2                                                                       CH.sub.3 O                                                  c3        CH.sub.3 CH.sub.2                                                                        ##STR26##                                                  c4        CH.sub.3 CH.sub.2                                                                        ##STR27##                                                  c5        CH.sub.3 CH.sub.2                                                                        ##STR28##                                                  ______________________________________                                    

                                      TABLE 1                                      __________________________________________________________________________     O-Chloromethyl S-Alkyl or S-Aryl Carbonothioates 4 Prepared                                                   IR (CHCl.sub.3).sup.d                            Product                                                                             Method                                                                              (%)Yield.sup.a                                                                     mbarb.p. (°C.)                                                                (%)Purity.sup.b                                                                    Formula.sup.cMolecular                                                                ##STR29##                                      __________________________________________________________________________     4a   B    41  62-66/17                                                                             90  C.sub.3 H.sub.5 ClO.sub.2 S                                                           1725                                                                    (140.6)                                                4b   A    81  67-70/14                                                                             95  C.sub.4 H.sub.7 ClO.sub.2 S                                                           1720                                                                    (154.6)                                                4b   B    49        90                                                         4c   B    72  99-101/24                                                                            84  C.sub.6 H.sub.11 ClO.sub.2 S                                                          1720                                                                    (182.7)                                                4d   A    99  90-92/0.2                                                                            95  C.sub.8 H.sub.7 ClO.sub.2 S                                                           1740                                                                    (202.7)                                                4d   B    18        90                                                         4e   B    90  103-105/0.6                                                                          90  C.sub.9 H.sub.9 ClO.sub.2 S                                                           1722                                                                    (216.7)                                                __________________________________________________________________________      .sup.a Yield (unoptimized) of isolated product.                                .sup. b Estimated by .sup.1 HNMR.                                              .sup.c Satisfactory microanalyses obtained (C, H, S, Cl ± 0.4%).            .sup.d Recorded on a PerkinElmer 783 infrared spectrophotometer (10% in        CHCl.sub.3).                                                             

                  TABLE 2                                                          ______________________________________                                         .sup.1 H-NMR of Products 4 (CDCl.sub.3 /TMS)                                          ClCH.sub.2 O                                                            Product                                                                               (s, 2H)     R.sup.2                                                     ______________________________________                                         4a.sup.a                                                                              5.78        2.40 (s, 3H, CH.sub.3)                                      4b.sup.b                                                                              5.72        1.31 (t, 3H, J=7 Hz, CH.sub.3)                                                 2.90 (q, 2H, J=7 Hz, CH.sub.2)                              4c.sup.c                                                                              5.76        0.93 (t, 3H, J=7 Hz, CH.sub.3)                                                 1.2-1.8 (m, 4H, CH.sub.3  .sub.----CH.sub.2  .sub.----C                        H.sub.2)                                                                       2.92 (t, 2H, J=7 Hz, SCH.sub.2)                             4d.sup.b                                                                              5.70        7.50 (bs, 5H, Ph)                                           4e.sup.c                                                                              5.71        4.13 (s, 2H, CH.sub.2)                                                         7.29 (bs, 5H, Ph)                                           ______________________________________                                          .sup.a Recorded at 300 MHz on a Brucker AC300 spectrometer.                    .sup.b Recorded at 60 MHz on a Jeol PMX60 spectrometer.                        .sup.c Recorded at 100 MHz on a Jeol FX100 spectrometer.                 

                                      TABLE 3                                      __________________________________________________________________________     O-Iodomethyl S-Alkyl or S-Aryl Carbonothioates 5 Prepared                                                           IR (CHCl.sub.3).sup.d                      Product                                                                             Yield.sup.a (%)                                                                      Isolated NaCl (%)                                                                        Purity.sup.b (%)                                                                     Molecular Formula.sup.c                                                                  ##STR30##                                __________________________________________________________________________     5a   96    96              C.sub.3 H.sub.5 IO.sub.2 S                                                     (232.0)                                             5b   96    95        90    C.sub.4 H.sub.7 IO.sub.2 S                                                               1720                                                                 (246.1)                                             5b.sup.e                                                                            94              95-100                                                    5c   97    98              C.sub.6 H.sub.11 IO.sub.2 S                                                    (274.1)                                             5d   95    94        95    C.sub.8 H.sub.7 IO.sub.2 S                                                     (294.1)                                             5e   97    96              C.sub.9 H.sub.9 IO.sub.2 S                                                     (308.1)                                             __________________________________________________________________________      .sup.a Yield (unoptimized) of isolated product (not distilled).                .sup.b Estimated by .sup.1 HNMR.                                               .sup.c No microanalyses obtained.                                              .sup.d Recorded on a Perkin Elmer 783 infrared spectrophotometer (10% in       CHCl.sub.3)                                                                    .sup.e Optimized method.                                                 

                  TABLE 4                                                          ______________________________________                                         .sup.1 H-NMR of Products 5 (CDCl.sub.3 /TMS).sup.a                                      JCH.sub.2 O                                                           Product  (s, 2 H)    R.sup.2                                                   ______________________________________                                         5b       5.98        1.31(t, 3H, J=7-8Hz, CH.sub.3)                                                 1.92(q, 2H, J=7-8Hz, CH.sub.2)                            5d       5.95        7.10-7.90(m, 5H, Ph)                                      ______________________________________                                          .sup.a Recorded at 60 MHz on a Jeol PMX60 spectrometer                   

                                      TABLE 5                                      __________________________________________________________________________     O-Acyloxymethyl S-Alkyl or S-Aryl Carbonothioates 6 Prepared                                                  IR (CHCl.sub.3).sup.c                            Product                                                                             Method                                                                              (%)Yield.sup.a                                                                     mbarb.p. (°C.)                                                                 (%)Purity.sup.b                                                                    FormulaMolecular                                                                      ##STR31##                                                                               ##STR32##                            __________________________________________________________________________     6ab.sup.d                                                                           C    53  52-54/0.4                                                                             80  C.sub.5 H.sub.8 O.sub.4 S.sup.e                                                       1735     (Broad)                                                        (164.2)                                               6ba  C    48  54-55/0.4                                                                             90  C.sub.5 H.sub.8 O.sub.4 S.sup.e                                                       1720     1760                                                           (164.2)                                               6bb  C    64  62-64/0.5                                                                             75  C.sub.6 H.sub.10 O.sub.4 S.sup.e                                                      1720     1765                                                           (178.2)                                               6bb  F    17  50/0.3 90  .sup.f                                                6ca  C    43  58/0.4 85  C.sub.6 H.sub.10 O.sub.4 S.sup.f,g                                                    1720     1760                                                           (178.2)                                               6cb  C    70  72-74/0.3                                                                             90  C.sub.7 H.sub.12 O.sub.4 S.sup.f,h                                                    1720     1760                                                           (192.2)                                               6cb  D.sup.i,j                                                                           98  71-73/0.3                                                                             95-100                                                                             .sup.e                                                6cc  C    50  87/0.5 70  C.sub.9 H.sub.16 O.sub.4 S.sup.k                                                      1720     1760                                                           (220.3)                                               6da  C    98  68-70/0.6                                                                             90  C.sub.7 H.sub.12 O.sub.4 S.sup.e                                                      1722     1760                                                           (192.2)                                               6db  C    76  75-80/0.5                                                                             95  C.sub.8 H.sub.14 O.sub.4 S.sup.e                                                      1720     1760                                                           (206.2)                                               6db  D.sup.i                                                                             92         95                                                        6db  J    87         80-85                                                     6dd  C    72  113-130/0.4.sup.l                                                                     85  C.sub.12 H.sub.14 O.sub.4 S.sup.e                                                     1735     1760 (shoulder)                                                (254.3)                                               6eb  C    66  80-84/0.2                                                                             75  C.sub.9 H.sub.16 O.sub.4 S.sup.e                                                      1720     1760                                                           (220.3)                                               6fb  C    65  66-68/0.4                                                                             90  C.sub.9 H.sub.16 O.sub.4 S.sup.m                                                      1720     1750                                                           (220.3)                                               6fc  C    72  90-92/0.6                                                                             90  C.sub.11 H.sub.20 O.sub.4 S.sup.f,h                                                   1720     1750                                                           (248.3)                                               6fe  C    69  136-140/0.3                                                                           90  C.sub.14 H.sub. 18 O.sub.4 S.sup.f,o                                                  1720     1750                                                           (282.4)                                               6gb  C    62  92-96/0.3                                                                             90  C.sub.10 H.sub.18 O.sub.4 S.sup.e                                                     1720     1755                                                           (234.3)                                               6hb  D.sup.p                                                                             85  98-104/0.3                                                                            85  C.sub.11 H.sub.20 O.sub.4 S.sup.e                                                     1720     1755                                                           (248.3)                                               6ib  D.sup.p                                                                             78         90  C.sub.12 H.sub.22 O.sub.4 S.sup.e                                                     1720     1755                                                           (262.4)                                               6jb  D.sup.p                                                                             87         80  C.sub.13 H.sub.24 O.sub.4 S.sup.e                                                     1720     1755                                                           (276.4)                                               6kb  E    99         80  C.sub.18 H.sub.34 O.sub.4 S.sup.k                                                     1720     1760                                                           (346.5)                                               6kb  D.sup.p                                                                             94         95                                                        6lb  C    64  122-24/0.2                                                                            90  C.sub.11 H.sub.12 O.sub.4 S.sup.f                                                     1725     1740                                                           (240.3)                                                                               (shoulder)                                     6mb  D.sup.i                                                                             74  37.2-38.4.sup.q                                                                       95  C.sub.9 H.sub.10 O.sub.5 S.sup.f                                                      1720     1740                                                           (230.2)                                               6nb.sup.d                                                                           C    54  110-14/0.3                                                                            90  C.sub.7 H.sub.12 O.sub.5 S.sup.f,r                                                    1720     1760                                                           (208.2)                                               6ob  C    28  90-94/0.3                                                                             90  C.sub.7 H.sub.10 O.sub.5 S.sup.f                                                      1720     1755                                                           (206.2)         (1740 α-keto)                   6ob  D.sup.i                                                                             50         90  .sup.e                                                6pb  D.sup.i                                                                             75  130-140/0.4                                                                           90  C.sub.9 H.sub.14 O.sub.5 S.sup.f                                                      1720     1760                                                           (234.3)                                                                               (broad)                                        6qb  D.sup.s                                                                             34  91/0.1 90  C.sub.8 H.sub.14 O.sub.5 S.sup.e                                                      1720     1780                                                           (222.3)                                               6rb  D.sup.i                                                                             95  49-50.sup.q                                                                           99  C.sub.12 H.sub.14 O.sub.5 S.sup.f                                                     1720     1780                                                           (270.3)                                               6sb.sup.d                                                                           F    42  40/0.3 75  C.sub.6 H.sub.7 F.sub.3 O.sub.4 S.sup.e                                               1725     1805                                                           (232.2)                                               6tb.sup.d                                                                           F    46         90  C.sub.8 H.sub.13 NO.sub.5 S.sup.e                                                     1720     1760                                                           (235.3)         (1680 amide)                          6ub.sup.d                                                                           D.sup.i                                                                             62  81.5-83.sup.q                                                                         95  C.sub.12 H.sub.17 NO.sub.7 S.sub.2 .sup.f                                             1720     1780                                                           (351.4)         (1800 β-lactam)                  __________________________________________________________________________      .sup.a Yield (unoptimized) of isolated product.                                .sup.b Estimated by .sup. 1 HNMR.                                              .sup.c Recorded on a Perkin Elmer 783 infrared spectrophotometer (10% in       CHCl.sub.3).                                                                   .sup.d Not transformed into the derived carbonochloridate 7.                   .sup.e Not analysed.                                                           .sup.f Satisfactory microanalyses obtained (C, H, S (N) ± 0.4%).            .sup.g (C: +1.0%, S: -1.7%).                                                   .sup.h (S: -0.7%).                                                             .sup.i Organic phase: methylene chloride.                                      .sup.j Optimized method.                                                       .sup.k Unsatisfactory microanalyses obtained.                                  .sup.l Product decomposes during distillation.                                 .sup.m Purified by column chromatography on SiO.sub.2 (Merck 60,               nhexane/ethyl acetate, 9:1) to obtain satisfactory microanalyses.              .sup.n (C: +0.65%; S: +1.00%).                                                 .sup.o (C: -0.6%; S: +0.45).                                                   .sup.p Organic phase: ethyl acetate.                                           .sup.q Melting point, uncorrected, obtained on a Buchi 510 apparatus.          .sup.r (C: +0.45%).                                                            .sup.s Organic phase: ethylene chloride.                                 

                                      TABLE 6                                      __________________________________________________________________________     .sup.1 H-NMR of Products 6 (CDCl.sub.3 /TMS).                                                       OCH.sub.2 O                                               Product                                                                             R.sup.1         (s, 2H)                                                                              R.sup.2                                             __________________________________________________________________________     6ab.sup.a                                                                           8.05 (s, 1H, H) 5.85  1.32 (t, 3H, J=7.5 Hz, CH.sub.3)                                               2.92 (q, 2H, J=7.5 Hz, CH.sub.2)                    6ba.sup.b                                                                           2.12 (s, 3H, CH.sub.3)                                                                         5.79  2.37 (s, 3H, CH.sub.3)                              6bb.sup.b                                                                           2.12 (s, 3H, CH.sub.3)                                                                         5.79  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                                               2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                    6ca.sup.b                                                                           1.16 (t, 3H, J=7.5 Hz, CH.sub.3)                                                               5.81  2.36 (s, 3H, CH.sub.3)                                   2.40 (q, 2H, J=7.5 Hz, CH.sub.2)                                          6cb.sup.a                                                                           1.16 (t, 3H, J=7.5 Hz, CH.sub.3)                                                               5.81  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                         2.40 (q, 2H, J=7.5 Hz, CH.sub.2)                                                                     2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                    6cc.sup.b                                                                           1.16 (t, 3H, J=7.5 Hz, CH.sub.3)                                                               5.80  0.93 (t, 3H, J=7 Hz, CH.sub.3)                           2.40 (q, 2H, J=7.5 Hz, CH.sub.2)                                                                     1.2-1.8 (m, 4H, CH.sub.3  .sub.----CH.sub.2                                    .sub.----CH.sub.2)                                                             2.89 (t, 2H, J=7 Hz, CH.sub.2 S)                    6da.sup.b                                                                           0.96 (t, 3H, J=7 Hz, CH.sub.3)                                                                 5.81  2.36 (s, 3H, CH.sub.3)                                   1.5-1.9 (m, 2H, CH.sub.3  .sub.----CH.sub.2 CH.sub.2)                          2.3 (m, 2H, COCH.sub.2)                                                   6db.sup.a                                                                           0.96 (t, 3H, J=7 Hz, CH.sub.3)                                                                 5.77  1.30 (t, 3H, J=7.5 Hz, CH.sub.3)                         1.7 (m, 2H, CH.sub.3  .sub.----CH.sub.2 CH.sub.2)                                                    2.88 (q, 2H, J=7.5 Hz, CH.sub.2)                         2.35 (t, 2H, J=7 Hz, COCH.sub.2)                                          6dd.sup.a                                                                           0.95 (t, 3H, J=7 Hz, CH.sub.3)                                                                 5.89  7.1-7.8 (m, 5H, Ph)                                      1.3-2.0 (m, 2H, CH.sub.3  .sub.----CH.sub.2 CH.sub.2)                          2.35 (t, 2H, J=7 Hz, COCH.sub.2)                                          6eb.sup.a                                                                           0.8-2.0 (m, 7H,  .sub. ----CH.sub.3  .sub.----CH.sub.2  .sub.----CH.s          ub.2)           5.79  1.31 3H, J=7.5 Hz, CH.sub.3)                             2.39 (t, 2H, J=7 Hz, COCH.sub.2)                                                                     2.91 (q, 2H, J=7.5 Hz, CH.sub.2)                    6fb.sup.a                                                                           1.25 (s, 9H, (CH.sub.3).sub.3 C)                                                               5.80  1.31 (t, 3H, J=7.5 Hz, CH.sub.3)                                               2.91 (q, 2H, J=7.5 Hz, CH.sub.2)                    6fc.sup.b                                                                           1.22 (s, 9H, (CH.sub.3).sub.3 C)                                                               5.80  0.92 (t, 3H, J=7 Hz, CH.sub.3)                                                 1.2-1.9 (m, 4H, CH.sub.3  .sub.----CH.sub.2                                    .sub.----CH.sub.2)                                                             2.88 (t, 2H, J=7 Hz, CH.sub.2 S)                    6fe.sup.b                                                                           1.20 (s, 9H, (CH.sub.3).sub.3 C)                                                               5.79  4.11 (s, 2H, CH.sub.2)                                                         7.29 (bs, 5H, Ph)                                   6gb.sup.a                                                                           0.8-2.0 (m, 6H, CH.sub.3  .sub.----CH.sub.2  .sub.----CH.sub.2                 .sub.----CH.sub.2                                                                              5.79  1.32 (t, 3H, J=7.5 Hz, CH.sub.3)                         0.9 (t, 3H, J=7 Hz, CH.sub.3)                                                                        2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                         2.38 (t, 2H, J=7 Hz, COCH.sub.2)                                          6hb.sup.a                                                                           0.7-2.0 (m, 8H, CH.sub.3 ( .sub.----CH.sub.2).sub.4)                                           5.80  1.31 (t, 3H, J=7.5 Hz, CH.sub.3)                         0.9 (t, 3H, J=7 Hz, CH.sub.3)                                                                        2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                         2.35 (t, 2H, J=7 Hz, COCH.sub.2)                                          6ib.sup.a                                                                           0.7-2.0 (m, 10H, CH.sub.3 ( .sub.----CH.sub.2).sub.5                                           5.80  1.30 (t, 3H, J=7.5 Hz, CH.sub.3)                         0.9 (t, 3H, J=7 Hz, CH.sub.3)                                                                        2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                         2.38 (t, 2H, J=7 Hz, COCH.sub.2)                                          6jb.sup.b                                                                           0.88 (bt, 3H, CH.sub.3                                                                         5.80  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                         1.27 (m, 10H, CH.sub.3 ( .sub.----CH.sub.2).sub.5)                                                   2.89 (q, 2H, J=7.5 Hz, CH.sub.2)                         1.60 (m, 2H,  .sub.----CH.sub.2 CH.sub.2 CO)                                   2.37 (t, 2H, COCH.sub.2)                                                  6kb.sup.b                                                                           0.88 (bt, 3H, CH.sub.3)                                                                        5.80  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                         1.26 (m, 20H, CH.sub.3 ( .sub.----CH.sub.2).sub.10)                                                  2.89 (q, 2H, J=7.5 Hz, CH.sub.2)                         1.60 (m, 2H, CH.sub.2 CH.sub.2 CO)                                             2.37 (t, 2H, COCH.sub.2)                                                  6lb.sup.a                                                                           7.2-7.8 (m, 2H, arom)                                                                          6.01  1.30 (t, 3H, J=7.5 Hz, CH.sub.3)                         7.95-8.3 (m, 2H arom) 2.89 (q, 2H, J=7.5 Hz, CH.sub.2)                    6mb.sup.b                                                                           6.55 (m, 1H arom)                                                                              6.01  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                         7.3 (m, 1H arom)      2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                         7.65 (m, 1H arom)                                                         6nb.sup.a                                                                           1.41 (d, 3H, CH.sub.3)                                                                         5.85  1.32 (t, 3H, J=7.5 Hz, CH.sub.3)                         3.0 (bs, 1H, OH)      2.90 (q, 2H, 7=7.5 Hz, CH.sub.2)                         4.35 (bq, 1H, CH)                                                         bob.sup.b                                                                           2.50 (s, 3H, CH.sub.3)                                                                         5.93  1.34 (t, 3H, J=7.5 Hz, CH.sub.3)                                               2.91 (q, 2H, J=7.5 Hz, CH.sub.2)                    6pb.sup.a                                                                           2.16 (s, 3H, CH.sub.3)                                                                         5.79  1.31 (t, 3H, J=7.5 Hz, CH.sub.3)                         2.8 (m, 4H, ( .sub.----CH.sub.2).sub.2)                                                              2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                    6qb.sup.a                                                                           1.22 (t, 3H, J=7 Hz, CH.sub.3)                                                                 5.85  1.32 (t, 3H, J=7.5 Hz, CH.sub.3)                         3.6 (q, 2H, J=7 Hz, CH.sub.2 O)                                                                      2.91 (q, 2H, J=7.5 Hz, CH.sub.2)                         4.12 (s, 2H, OCH.sub.2 CO)                                                6rb.sup.a                                                                           4.65 (s, 2H, OCH.sub.2 CO)                                                                     5.85  1.32 (t, 3H, J=7.5 Hz, CH.sub.3)                         6.8-7.6 (m, 5H, Ph)   2.91 (q, 2H, J=7.5 Hz, CH.sub.2)                    6sb.sup.a            5.95  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                                               2.92 (q, 2H, J=7.5 Hz, CH.sub.2)                    6tb.sup.a                                                                           2.05 (s, 2H, CH.sub.3)                                                                         5.80  1.33 (t, 3H, J=7.5 Hz, CH.sub.3)                         4.08 (d, 2H, J=5 Hz, CH.sub.2)                                                                       2.90 (q, 2H, J=7.5 Hz, CH.sub.2)                         6.0-6.6 (m, 1H, NH)                                                       6ub.sup.b                                                                           1.42, .60 (2s, 3H each, 2CH.sub.3)                                                             5.78, 5.97                                                                           1.34 (t, 3H, J=7.5 Hz, CH.sub.3)                         3.40 (m, 2H, CH .sub.----CH.sub.2 CON),                                                        (ABq, 2H,                                                                            2.91 (q, 2H, J=7.5 Hz, CH.sub.2)                                         J=5.8 Hz)                                                      4.42 (s, 1H, (CH.sub.3).sub.2 C .sub.----CHCOO)                                4.63 (dd, 1H, J=2.8 and 3.7)                                                   SO.sub.2  .sub.----CHCH.sub.2)                                            __________________________________________________________________________      .sup.a Recorded at 60 MHz on a Jeol PMX60 spectrometer.                        .sup.b Recorded at 100 MHz on a Jeol FX100 spectrometer.                 

                                      TABLE 7                                      __________________________________________________________________________     Acyloxymethyl Carbonochloridates 7 Prepared                                                                       IR.sup.c                                     Product                                                                             Method                                                                              (%)Yield.sup.a                                                                     (%)Purity.sup.b                                                                    From                                                                               mbarb.p. (°C.)                                                                FormulaMolecular                                                                      ##STR33##                                                                               ##STR34##                         __________________________________________________________________________     7b   G    50  90  6ba 62/13 C.sub.4 H.sub.5 ClO.sub.4 .sup.d                                                      1785 (broad)                                                            (152.5)                                            7b   G    63  80  6bb 60-62/13                                                                             .sup.d                                             7c   G    31  85  6cb 72.5/16                                                                              C.sub.5 H.sub.7 ClO.sub.4 .sup.e,f                                                    1780 (broad)                                                            (166.0)                                            7c   H    86  95  6cb 70-71/13                                                                             .sup.e,g                                           7d   G    60  95  6da 82-84/13                                                                             C.sub.6 H.sub.9 ClO.sub.4 .sup.d                                                      1780 (broad)                                                            (180.6)                                            7d   G    91  90  6db 80-82/13                                                                             .sup.d                                             7d   G            6dd .sup. h                                                  7e   G    88  85  6eb 90-94/13                                                                             C.sub.7 H.sub.11 ClO.sub.4 .sup.d                                                     1780 (broad)                                                            (194.6)                                            7f   G    60  95  6fb 73-75/13                                                                             C.sub.7 H.sub.11 ClO.sub.4 .sup.d                                                     1785     1760                                                           (194.6)                                            7f   G.sup.i      6fc .sup.j                                                   7f   G.sup.i      6fe .sup.j                                                   7g   G    77  90  6gb 65-67/0.2                                                                            C.sub.8 H.sub.13 ClO.sub.4 .sup.d                                                     1780 (broad)                                                            (208.6)                                            7h   G    56  85  bhb 75-78/0.3                                                                            C.sub.7 H.sub.15 ClO.sub.4 .sup.d                                                     1780 (broad)                                                            (198.7)                                            7i   G    61  95  6ib 80-90/0.3                                                                            C.sub.10 H.sub.17 ClO.sub.4 .sup.d                                                    1780 (broad)                                                            (236.7)                                            7j   G    100 85  6jb       C.sub.11 H.sub.19 ClO.sub.4 .sup.d                                                    1780 (broad)                                                            (250.7)                                            7k   G    100 85  6kb       C.sub.16 H.sub.29 ClO.sub.4 .sup.d                                                    1780 (broad)                                                            (320.9)                                            7l   G    65  95  6lb 102-103/0.3                                                                          C.sub.9 H.sub.7 ClO.sub.4 .sup.e,k                                                    1780     1745                                                           (214.6)                                            7m   G.sup.i                                                                             96  85  6mb       C.sub.7 H.sub.7 ClO.sub.5 .sup.d                                                      1780     1750                                                           (204.6)                                            7o   G    70  85  6ob 80-90/0.3                                                                            C.sub.5 H.sub.5 ClO.sub.5 .sup.d                                                      1780     1760                                                           (180.5)         (1740 α-keto)                7p   G    28  75  6pb 110-20/1.3                                                                           C.sub.7 H.sub.9 ClO.sub.5 .sup.d                                                      1765 (broad)                                                            (208.6)                                                                               (1720 γ-keto)                         7q   G    48  80  6qb 78/0.3                                                                               C.sub.6 H.sub.9 ClO.sub.5 .sup.d                                                      1790                                                                    (196.6)                                            7r   G.sup.i,l                                                                           98  80  6rb       C.sub.10 H.sub.9 ClO.sub.5 .sup.d                                                     1790 (broad)                                                            (244.6)                                            __________________________________________________________________________      .sup.a Yield (unoptimized) of isolated product.                                .sup.b Estimated by .sup.1 HNMR.                                               .sup.c Recorded on a PerkinElmer 783 spectrophotometer (10% in                 CHCl.sub.3).                                                                   .sup.d Not analysed.                                                           .sup.e Satisfactory microanalyses obtained (C, H, Cl ± 0.4%).               .sup.f (S: +1.5%).                                                             .sup.g (S: +0.7%).                                                             .sup.h Not purifiable by distillation.                                         .sup.i Reaction in 10% CH.sub.2 Cl.sub.2 solution.                             .sup.j Not obtainable in a satisfactory purity.                                .sup.k (S: +0.95%).                                                            .sup.l Reaction in 10% CH.sub.3 CN solution.                             

                  TABLE 8                                                          ______________________________________                                         .sup.1 H-NMR of Products 7 (CDCl.sub.3 /TMS)                                                                 OCH.sub.2 O                                      Product   R.sup.1             (s, 2H)                                          ______________________________________                                         7b.sup.a  2.13 (s, 3H, CH.sub.3)                                                                             5.78                                             7c.sup.b  1.18 (t, 3H, J=7.5 Hz, CH.sub.3)                                                                   5.83                                                       2.38 (q, 2H, J=7.5 Hz, CH.sub.2)                                     7d.sup.b  0.98 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.82                                                       1.73 (m, 2H, CH.sub.3  .sub.----CH.sub.2)                                      2.47 (t, 2H, J=7 Hz, COCH.sub.2)                                     7e.sup.b  0.93 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.82                                                       1.2-1.9 (m, 4H, CH.sub.3 ( .sub.----CH.sub.2).sub.2)                           2.42 (t, 2H, J=7 Hz, COCH.sub.2)                                     7f.sup.a  1.22 (s, 9H, (CH.sub.2).sub.3 C)                                                                   5.81                                             7g.sup.a  0.90 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.80                                                       1.0-2.0 (m, 6H, CH.sub.3 ( .sub.----CH.sub.2).sub.3)                           2.40 (t, 2H, J=7 Hz, COCH.sub.2)                                     7h.sup.a  0.90 (t, 3H, J=7 Hz, CH.sub.3 )                                                                    5.83                                                       1.0-2.0 (m, 8H, CH.sub.3 ( .sub.----CH.sub.2).sub.4)                           2.45 (t, 2H, J=7 Hz, COCH.sub.2)                                     7i.sup.a  0.90 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.83                                                       1.0-2.0 (m, 10H, CH.sub.3 ( .sub.----CH.sub.2).sub.5)                          2.44 (t, 2H, J=7 Hz, COCH.sub.2)                                     7j.sup.a  0.90 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.83                                                       1.0-2.0 (m, 12H, CH.sub.3 ( .sub.----CH.sub.2).sub.6)                          2.44 (t, 2H, J=7 Hz, COCH.sub.2)                                     7k.sup.a  0.90 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.81                                                       0.8-2.0 (m, 22H, CH.sub.3 ( .sub.----CH.sub.2).sub.11)                         2.44 (t, 2H, J=7 Hz, COCH.sub.2)                                     7l.sup.a  7.2-77 (m, 3H arom) 6.03                                                       8.0-8.3 (m, 2H arom)                                                 7m.sup.a  6.6 (dd, 1H arom, J=4 and 2 Hz)                                                                    6.02                                                       7.32 (d, 1H arom, J=4 Hz)                                                      7.65 (bs, 1H arom)                                                   7o.sup.b  2.52 (s, 3H, CH.sub.3)                                                                             5.96                                             7p.sup.a  2.19 (s, 3H, CH.sub.3)                                                                             5.70                                                       2.75 (m,, 4H,  .sub.----CH.sub.2  .sub.----CH.sub.2)                 7q.sup.a  1.22 (t, 3H, J=7 Hz, CH.sub.3)                                                                     5.83                                                       3.60 (q, 2H, J=7 Hz, CH.sub.3  .sub.----CH.sub.2)                              4.15 (s, 2H, OCH.sub.2 CO)                                           7r.sup.a  4.7 (s, 2H, OCH.sub.2)                                                                             5.85                                                       6.7-7.6 (m, 5H, Ph)                                                  ______________________________________                                          .sup.a Recorded at 60 MHz on a Jeol PMX60 spectrometer                         .sup.b Recorded at 100 MHz on a Jeol PMX100 spectrometer                 

                                      TABLE 9                                      __________________________________________________________________________     Acylation Products 8 Prepared.                                                                                    IR(CHCl.sub.3).sup.c                         Product                                                                             Yield.sup.a (%)                                                                      b.p. (°C.) mbar                                                                 Purity.sup.b (%)                                                                     Molecular Formula                                                                        ##STR35##                                  __________________________________________________________________________     8cl.sup.d                                                                           31    90-91.sup.e                                                                            95    C.sub.11 H.sub.12 ClNO.sub.4 .sup.f                                                      1755 (broad)                                                         (257.7)                                               8cl.sup.g                                                                           71            95-100                                                      8c2.sup.h                                                                           62    55-56/0.3                                                                              90    C.sub.6 H.sub.10 O.sub.5 .sup.i                                                          1760 (broad)                                                         (162.1)                                               8c3.sup.h                                                                           49    66-68/0.5                                                                              95    C.sub.9 H.sub.16 O.sub.5 .sup.f                                                          1760 (broad)                                                         (204.2)                                               8c3.sup.j                                                                           .sup. 98.sup.k                                                                               95-100                                                      8c4.sup.h                                                                           36    120-22/0.3                                                                             85    C.sub.13 H.sub.16 O.sub.5 .sup.i                                                         1760 (broad)                                                         (252.31)                                              8c5.sup.h                                                                           61    35-36.sup.e                                                                            95-100                                                                               C.sub.11 H.sub.11 NO.sub.7 .sup.f                                                        1775 (broad)                                                         (269.21)                                              __________________________________________________________________________      .sup.a Yield of isolated product.                                              .sup.b Estimated by NMR.                                                       .sup.c Recorded on a Perkin Elmer 753 spectrophotometer (10% in                CHCl.sub.3).                                                                   ##STR36##                                                                      .sup.e Melting point, uncorrected, obtained on a Buchi 510 apparatur.          .sup.f Satisfactory microanalyses obtained (C, H, (Cl, N) + 0.4%).             ##STR37##                                                                      ##STR38##                                                                      .sup.i Not analysed.                                                           .sup.j Using molecular sieve as a HCl scavenger.                               .sup.k Not distilled.                                                    

                  TABLE 10                                                         ______________________________________                                         .sup.1 H-NMR of Products 8 (CDCl.sub.3 /TMS).                                  R.sup.1                                                                        CH.sub.3   CH.sub.2 CO                                                         (t, 3H)    (q, 2H)  OCH.sub.2 O                                                Product                                                                               J = 7.5 Hz   (s, 2H)  Nu                                                ______________________________________                                         8cl.sup.a                                                                             1.15    2.39     5.81   7.05 (bs, 1H, NH)                                                              7.25 (m, 4H arom)                               8c2.sup.a                                                                             1.16    2.40     5.76   3.83 (s, 3H, CH.sub.3)                          8c3.sup.a                                                                             1.16    2.40     5.76   0.93 (t, 3H, J=7 Hz,                                                            .sub.----CH.sub.3 CH.sub.2)                                                   1.29 (d, 3H, J=6 Hz,                                                            .sub.----CH.sub.3 CH)                                                         1.6 (m, 2H, CH.sub.2)                                                          4.74 (m, 1H, CH)                                8c4.sup.a                                                                             1.14    2.38     5.73   2.98 (t, 2H, J=7 Hz,                                                           Ph .sub.----CH.sub.2)                                                          4.37 (t, 2H, J=7 Hz,                                                           CH.sub.2  .sub.---- CH.sub.2 O)                                                7.25 (bs, 5H, Ph)                               8c5.sup.b                                                                             1.20    2.47     5.89   7.42 (m, 2H arom)                                                              8.30 (m, 2H arom)                               ______________________________________                                          .sup.a Recorded at 100 MHz on a Jeol FX10 spectrometer.                        .sup.b Recorded at 300 MHz on a Brucker AC300 spectrometer.              

EXAMPLE 1 (METHOD A) O-Chloromethyl S-Ethyl Carbonothioate (4b)

A solution of ethanethiol (37 mL, 500 mmol) and Et₃ N (Fluka, purum, 69.3 mL, 500 mmol) in Et₂ O (200 mL) is added during 2 h to a stirred solution of 3 (44.0 mL, 500 mmol) in Et₂ O (900 mL) at 0°-5° C. After stirring an additional 30 min. at 0°-5° C. and during the night at room temperature the resulting suspension is filtered. The filtrate is evaporated and the residue distilled to give 4b; yield: 57.9-62.6 g (75-81%), bp 67°-70° C./14 mbar.

EXAMPLE 2 (Method B) O-Chloromethyl S-n-Butyl Carbonothioate (4c)

To a stirred 1M solution of NaOMe in MeOH (100 mL) at 0°-5° C. is dropwise added n-butanethiol (10.7 mL, 100 mmol). After evaporation to dryness the residue is suspended in Et₂ O (200 mL) at -75° C. A solution of 3 (8.8 mL, 100 mmol) in Et₂ O (50 mL) is added dropwise during 1 h with stirring followed by stirring overnight at ambient temperature. Evaporation of the solvent after filtration furnishes crude product which distilled yields 13.2 g (72%) of 4c, bp 99°-101° C./24 mbar.

EXAMPLE 3 O-Iodomethyl S-Ethyl Carbonothioate (5b)

The ester 4 b (15.4 g, 100 mmol) is added to a solution of NaI (22.5 g, 150 mmol) in Me₂ CO (125 ml) and stirred for 3 h at 40° C. followed by filtration and washing with Me₂ CO and Et₂ O. The filtrate is evaporated and the residue partitioned (all solutions being ice-cold) between pentane (300 mL) and H₂ O (100 mL). The organic phase is washed with aqueous 5% NaHCO₃ (50 mL), 1% aqueous Na₂ S₂ O₃ (50 mL, or more until colourlessness is achieved), H₂ O (2×50 mL), dried (MgSO₄), and evaporated. Yield of crude product: 23.6 g (96%).

EXAMPLE 4 (Optimal procedure

The Procedure of Example 3 is slightly modified by increasing the amount of NaI to 30 g (200 ml), adding NaHCO₃ (0.8 g, 10 mmol), and heating at 40° C. for 4 h. Yield: 23.1 g (94%).

EXAMPLE 5 (Method C) O-Butanoyloxymethyl S-Ethyl Carbonothioate (6db)

Crude 5b (23.6 g, 96 mmol) is added during 30 min to a stirred suspension of sodium butanoate (10.5 g, 96 mmol) in dry DMF (125 mL) at -20° C. followed by stirring overnight at ambient temperature. After filtration and washing with DMF (5 mL) and Et₂ O (10 mL),Et₂ O (250 mL) and ice-cold H₂ O (100 mL) are added to the combined filtrates. The aqueous phase is separated and extracted with Et₂ O (100 mL). The combined organic phases are washed (all solutions ice-cold) with 5% aqueous NaHCO₃ (50 mL), H₂ O (50 mL), 0.01N HCl (100 mL), and H₂ O (2×50 mL). After drying (MgSO₄) and evaporation of solvents the residue is distilled to yield 15.0 g (76%) of 6db, bp 75°-80° C./0.5 mbar.

EXAMPLE 6 (Method D) O-(2-Furancarbonyloxymethyl) S-Ethyl Carbonothioate (6mb)

2-Furancarboxylic acid (5.6 g, 50 mmol) is added to a stirred solution of NaHCO₃ (8.4 g, 100 mmol) and TBA HSO₄ (17.0 g, 50 mmol) in H₂ O (100 mL) at room temperature. After stirring for 10 min 1,2-dichloroethane (100 mL) is added and the stirring continued for 30 min. 5b (12.5 g, 50 mmol) in 1,2-dichloroethane (25 mL) is added over 15 min. The mixture is stirred for 60 min at room temperature. The organic phase is separated, washed with H₂ O (50 mL), dried (MgSO₄), and evaporated. The residue is stirred with Et₂ O (100 mL), insoluble material filtered off and washed with Et₂ O. The combined Et₂ O-phases are evaporated and the residue crystallized from ice-cold pentane to yield 8.5 g (74%) of 6mb, mp 37.2°-38.4° C.

EXAMPLE 7 (Method D O-Propanoyloxymethyl S-Ethyl Carbonothioate (6cb)

To a stirred solution of NaHCO₃ (45 g, 536 mmol) in H₂ O (540 ml) is added TBA HSO₄ (91.2 g, 268 mmol), propanoic acid (20.1 mL, 268 mmol), and CH₂ Cl₂ (540 ml). Following stirring for 1 h at room temperature a solution of 5b (49.2 g, 200 mmol) in CH₂ Cl₂ (100 mL) is added during 45 min keeping the temperature below 30° C. The stirring is continued for 11/2 h. The organic phase is separated, washed with H₂ O (200 mL), dried (MgSO₄), and evaporated. The residue is stirred in Et₂ O (800 mL) during the night, filtered, and washed with Et₂ O (50 mL). The filtrate is evaporated and distilled to yield 38.0 g (98%) of 6cb, bp 71°-73° C./0.3 mbar.

EXAMPLE 8 (Method D) O-(2-Oxopropanoyloxymethyl) S-Ethyl Carbonothioate (6ob)

Redistilled 2-oxopropanoic acid (12.6 ml, 0.18 mol) is added to a vigorously stirred mixture of NaHCO₃ (30.6 g, 0.36 mol), TBA HSO₄ (61.2 g, 0.18 mol), H₂ O (360 mL), and CH₂ Cl₂ (360 mL) in an open Erlenmeyer flask. Following stirring for 10 min 5b (44.0 g, 0.18 mol) in CH₂ Cl₂ (400 mL) is added during 3 h at 25° C. together with CH₂ Cl₂ (500 mL) in portions to compensate for the evaporation. In this way the formation of sulfurous by-products is minimized. The mixture is extracted with CH₂ Cl₂ (300-200 mL). The combined organic phases are washed with H₂ O (2×200 mL); dried (MgSO₄) and evaporated. The residue is triturated with Et₂ O (600 mL). After filtration the filtrate is treated with charcoal, evaporated, and the residue crystallized from pentane at -70° C. to yield 6ob, melting below room temperature.

EXAMPLE 9 (Method D) O-Tetradecanoyoxymethyl S-Ethyl Carbonothioate (6kb)

A THF solution (20 mL) of TBA tetradecanoate (8.4 g, 18 mmol), prepared by freeze-drying an aqueous solution of equimolar TBA OH and tetradecanoic acid, is slowly (30 min) added to a stirred solution of 5b (4.5 g, 18 mmol) in THF (20 mL) at room temperature. Following stirring during the night the precipitate formed is removed by filtration and washed with THF (5 mL). The filtrate is evaporated and the residue triturated with Et₂ O (100 mL) and filtered. The filtrate leaves 6.2 g (99%) impure (80% by ¹ H-NMR) oily product after evaporation.

EXAMPLE 10 (Method F) O-(N-Acetylglycyl)oxymethyl S-Ethyl Carbonothioate (6tb)

Finely powdered potassium N-acetylglycinate (5.8 g, 37 mmol) and TBA I (1.2 g, 3.4 mmol) are thoroughly mixed and shaken for 5 min with 5b (8.3 g, 34 mmol). The mixture is left for 48 h at room temperature and then extracted with Et₂ O (4×40 mL). The combined extracts are filtered and evaporated. The residue (6.4 g) is thoroughly extracted with pentane (4×25 mL) to remove unreacted 5b. The residue is freed from remaining traces of pentane by evaporation leaving 3.7 g of 6tb (46%).

EXAMPLE 11 (Method G) Butanoyloxymethyl Carbonochloridate (7d)

Redistilled SO₂ Cl₂ (5.85 mL, 72 mmol) is added to 6db (14.8 g, 72 mmol) at 0°-5° C. with stirring during 15 min followed by stirring at room temperature (45 min). Evaporation at room temperature and 20 mbar during the night and distillation yields 11.8 g (91%)of 7d, bp 80°-82° C./13 mbar.

EXAMPLE 12 (Method H) Propanoyloxymethyl Carbonochloridate (7c)

Redistilled SO₂ Cl₂ (5.7 mL, 70 mmol) is added at once to 6cb (13.5 g, 70 mmol) at -25°-30° C. with stirring. After stirring at this temperature for 10 min BF₃.OEt₂ (0.3 mL) is added followed by stirring at 0° C. (1 h) and at room temperature (30 min). Evaporation at room temperature and 20 mbar (about 1 h) and subsequent distillation yields 10.0 g (86%) of 7c, bp 70°-71° C./13 mbar.

EXAMPLE 13 O-1-Chloroethyl S-Ethyl Carbonothioate

By following the procedure of Method A but replacing 3 by 1-chloroethyl carbonochloridate a 75% yield of the title compound is obtained with bp 71°-73° C./13 mbar. C₅ H₉ ClO₂ S calc. C 35.61 H 5.40 Cl 21.02 S 19.01 (168.6) found 36.11 5.50 21.20 18.22 IR (10% CHCl₃): ν=1715 cm⁻¹. NMR (CDCl₃ /TMS)⁴⁴ : δ=1.31 (t, 3H, J=7 Hz, CH₃ CH₂); 1.78 (d, 3H, J=6 Hz, CH₃ CH); 2.90 (q, 2H, J=7 Hz, CH₂); 6.57 (q, 1H, J=6 Hz, CH).

EXAMPLE 14 (Method J) O-1-Butanoyloxyethyl S-Ethyl Carbonothioate

To a stirred solution of TBA butanoate (32.9 g, 100 mmol), prepared by freeze-drying an aqueous solution of equimolar TBA OH and butanoic acid, in THF (500 ml) is added O1-chloroethyl S-ethyl carbonate (16.9 g, 100 mmol) at room temperature. Following stirring for 4 d and evaporation the residue is partioned between ice-cold Et₂ O (600 mL) and H₂ O (100 mL). The organic phase is extracted with H₂ o (2×75 mL), dried (MgSO₄) and evaporated. The residue is distilled to yield 14.3 g (68%) of the title compound, bp 69°-72° C./0.3 mbar. C₉ H₁₆ O₄ S calc. C 49.07 H 7.32 S 14.55 (220.3) found 48.73 7.38 14.94 IR (10% CHCl₃): ν=1750 cm⁻¹. NMR (CDCl₃ /TMS)⁴⁴ : δ=0.98 (t, 3H, J=7 Hz, CH₃ (CH₂ )₂); 1.31 (t, 3H, J=7.5 Hz, CH₃ CH₂ S); 1.48 (d, 3H, J=5 Hz, CH₃ CH); 1.5-2.0 (m, 2H, CH₃ CH₂ CH₂); 2.31 (t, 2H, J=7 Hz, CH₂ CO); 2.88 (q, 2H, J=7.5 Hz, CH₂ S); 6.92 (q, 1H, J=5 Hz, CH).

EXAMPLE 15 1-Butanoyloxyethyl Carbonochloridate

Redistilled SO₂ Cl₂ (0.2 mL, 2.5 mmol) is added to O-1-butanoyloxyethyl S-ethylcarbonothioate (0.55 g, 2.5 mmol) at -40° C. The temperature is slowly (0.5 h) raised to 0° C. followed by the addition of CCl₄ (5 mL) and BF₃.OEt₂ (3 drops). After stirring at 0° C. for 1 h CCl₄ (5 mL) is added and the solution half-way evaporated. Addition of CCl₄ (5 mL) and half-way evaporation is repeated three times to leave the title compound (80% purity by ¹ H-NMR) only stable in solution. IR (10% CCl₄): ν=1760 cm⁻¹. ¹ H-NMR (CDCl₃ :CCl₄ (1:1)/TMS)⁴⁵ : δ=0.98 (t, 3H, J=7.5 Hz, CH₃ (CH₂)₂); 1.57 (d, 3H, J=5.5 Hz, CH₃ CH); 1.6 (m, 2H, CH₃ CH₂ CH₂); 2.34 (t, 2H J=7.5 Hz, CH₂ CO); 6.80 (q, 1H, J=5.5 Hz, CH).

EXAMPLE 16 Sec-Butyl Propanoyloxymethyl Carbonate (8c3)

To a solution of 2-butanol (0.92 mL, 10 mmol) and 4-methylmorpholine (1.1 mL, 10 mmol) in CHCl₃ (20 mL) at -70° C. is added 7c (1.7 g, 10 mmol) during 20 min with stirring. The temperature is kept at -70° C. for 1 h and then raised (1 h) to room temperature. Next day following evaporation the residue is triturated with Et₂ O (25 mL) and filtered. The filtrate is evaporated and distilled to give 1.0 g (50%) of the title compound with bp 66°-68° C./5 mbar.

EXAMPLE 17 4-Nitrophenyl Propionyloxymethyl Carbonate (8c5)

4-Methylmorpholine (0.67 mL, 6.0 mmol) is added to a suspension of 4-nitrophenol (0.83 g, 6.0 mmol) in CH₂ Cl₂ (10 mL) with stirring. A solution of 7c (1.27 g, 95% purity, 7.2 mmol) in CH₂ Cl₂ (3 mL) is added during 20 min followed by stirring at 0° C. (30 min) and overnight at room temperature. After filtration the filtrate is evaporated and the residue partitioned between ice-cold Et₂ O (25 mL) and H₂ O (25 mL). The organic phase is extracted with ice-cold 0.5N NaOH (10 mL), H₂ O (3×15 mL), dried (MgSO₄) and evaporated. The residue (1.50 g) is extracted with hexane (2×10 mL) to leave the title compound (0.98 g, 61%), mp 35°-36° C.

EXAMPLE 18 Propanoyloxymethyl 4-Chlorophenylcarbamate (8cl)

Me₃ SiCl (2.3 mL, 18 mmol) is added to 4-chloroaniline (4.6 g, 36 mmol) in Et₂ O (50 mL) at room temperature with stirring during 20 min. Following an additional 30 min Stirring 7c (4.05 g, purity 90%, 22 mmol) in Et₂ O (30 mL) is slowly (1 h) added. The stirring is continued overnight. The precipitate is filtered off and the filtrate extracted with ice-cold 0.1N HCl (50 mL), H₂ O (3×50 mL), dried (MgSO₄) and evaporated. The residue (4.9 g) is extracted with hexane (50 mL) to leave 3.3 g (71%) of the title compound, mp 90°-91° C.

EXAMPLE 19 1-Butanoyloxyethyl 4-Chlorophenylcarbamate

A solution of 1-butanoyloxyethyl carbonochloridate (5 mmol) in CHCl₃ (10 mL) prepared as above but substituting CHCl₃ for CCl₄ is added to a solution of 4-chloroaniline (1.3 g, 10 mmol) in Et₂ O (40 mL) at -70° C. Following stirring for 2 h at -70° C. and 3 h at -40° C. the mixture is kept at -20° C. for 3d. After filtration, treatment of the filtrate with charcoal, and evaporation of the filtrate the residue is triturated with ice-cold pentane (15 mL) and recrystallized from pentane (70 mL) to yield 0.4 g (28%) of the title compound with mp 52°-54° C. C₁₃ H₁₆ ClNO₄ calc. C 54.65 H 5.64 Cl 12.41 N 4.90 (285.7) found 54.72 5.64 12.31 4.83 IR (10% CHCl₃): ν=1750 cm⁻¹. ¹ H-NMR (CDCl₃ /TMS)⁴⁵ : δ=0.95 (t, 3H, J=7 Hz, CH₃ (CH₂)₂ CO); 1.50 (d, 3H, J=5.5 Hz, CH₃ CH); 1.7 (m, 2H, CH₃ CH₂ CH₂ CO); 2.31 (t, 2H, J=7 Hz, CH₂ CO); 6.8 (bs, 1H, NH); 6.91 (q, 1H, J=5.5 Hz, CHCH₃); 7.28 (m, 4H arom.)

EXAMPLE 20 Sec-Butyl Propanoyloxymethyl Carbonate (8c3)

A mixture of 2-butanol (0.092 mL, 1 mmol), 7c (0.17 g, 1 mmol), and powdered molecular sieve (0.15 g, 4Å) in alcohol-free CHCl₃ (2 mL) is refluxed for 18 h. Following filtration through filter-aid and evaporation 0.2 g (98%) of the title compound is obtained.

EXAMPLE 21 D, L-N-Butanoyloxymethyleneoxycarbonyl-3,4-dihydroxyphenylalanine, dicyclohexylammonium salt ##STR39##

A mixture of 3-(3,4-dihydroxyphenyl)-D,L-alanine (2.0 g; 10 mmol), hexamethyldisilazane (7.36 ml; 40 mmol) and trimethylchlorosilane (4 drops), was heated at 120° C. for 3 hours under nitrogen. Excess of hexamethyldisilazane was distilled off in vacuo at 70° C./10 mmHg, in the end with xylene as a cosolvent to give A. ##STR40##

To A (10 mmol) in chloroform (15 ml) at -70° C. was added butanoyloxymethyl carbonochloridate (1.8 g, 10 mmol) in chloroform (5 ml). The temperature was slowly (over 2 hours) raised to 20° C., and the mixture stirred at 20° C. for hours. Then 5% extra butanoyloxymethyl carbonochloridate (˜100 mg) was added, the mixture stirred at 20° C. for 3.5 hours and evaporated in vacuo. The residue was dissolved in tertiary butanol (100 ml), hydrolysed with water (10 ml) for 20 minutes, dried with MgSO₄ and evaporated in vacuo.

The residue was extracted twice with ether (100+50 ml) for 72 hours. The extracts were evaporated in vacuo to give 3.3 g of B. ##STR41##

To a filtered solution of B (3.0 g; 8.8 mmol) in isopropyl ether (50 ml) at 0° C. was added dicyclohexylamine (1.75 ml; 8.8 mmol). The mixture was stirred at 0° C. for 15 minutes, the precipitate collected, washed with isopropyl ether (3×10 ml) and recrystallized first from acetone-ether (15/25 ml), then from acetone (40 ml) (60° C./0° C.) to yield 1.2 g (23%) of the title compound C with Mp: 135° C. 

What we claim is:
 1. An intermediate for the preparation of prodrugs, the intermediate having the formula I ##STR42## where R¹ stands for hydrogen or a straight or branched aliphatic C₁ -C₂₀ carbon chain or an aryl or aralkyl group or a heterocyclic or heterocyclic alkyl group wherein the heterocyclic group is selected from the group consisting of furyl, thienyl, pyrdrolyl, imidazolyl, thiazolyl, oxazolyl, pyridyl and pyrimidinyl and R³ is hydrogen or C₁ -C₃ alkyl; R¹ unsubstituted or being substituted by hydroxy or halogen, and its chain being is uninterrupted or interrupted by oxygen, or by carbonyl group(s); and R³ stands for hydrogen or C₁ -C₃ alkyl.
 2. An intermediate of formula I according to claim 1, in which R³ stands for hydrogen.
 3. An intermediate of formula I according to claim 1, in which R¹ stands for an aromatic or heterocyclic substituent selected from the group consisting of phenyl, furyl, thienyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, pyridyl, and pyrimidinyl.
 4. An intermediate according to claim 1, selected from the group consisting ofa) acetyloxymethyl carbonochloridate, b) propanoyloxymethyl carbonochloridate, c) butanoyloxymethyl carbonochloridate, d) pentanoyloxymethyl carbonochloridate, c) benzoyloxymethyl carbonochloridate.
 5. Method for producing an intermediate having formula I as follows: ##STR43## where R¹ stands for hydrogen or a straight or branched aliphatic C₁ -C₂₀ carbon chain or an aryl or aralkyl group or a heterocyclic or heterocyclic alkyl group wherein the heterocyclic group is selected from the group consisting of furyl, thienyl, pyrdrolyl, imidazolyl, thiazolyl, oxazolyl pyridyl or pyrimidnyl, comprising, reacting a 1-haloalkyl carbonochloridate derivative of the formula IV ##STR44## where R³ is hydrogen or C₁ -C₃ alkyl,with R² SR⁴, where R² is C₁ -C₄ alkyl, and R⁴ is hydrogen or an alkali metal ion, to form a 1-haloalkyl carbonothioate of the formula V ##STR45## R² and R³ having the above meanings, transforming the formed 1-haloalkyl carbonothioate into a 1-acyloxyalkyl carbonothioate of the formula VI ##STR46## R¹, R² and R³ having the above meanings, through a reaction with a salt of a carboxylic acid R¹ COOH, R¹ having the above meanings, and finally reacting the 1-acyloxyalkyl carbothioate of formula VI with a chlorinating agent to yield the desired intermediate of formula I.
 6. A method according to claim 5, wherein a compound according to formula I wherein R³ is hydrogen, is prepared which comprises converting the compound of formula V to the corresponding iodide by reaction with sodium iodide, before transforming it via VI to I.
 7. A method according to claim 5 or 6, in which the chlorinating agent is sulfuryl chloride. 